Search on: STRIATONIGRAL DEGENERATION 
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Descriptor English:   Striatonigral Degeneration 
Descriptor Spanish:   Degeneración Estriatonigral 
Descriptor Portuguese:   Degeneração Estriatonigral 
Tree Number:   C10.177.575.550.875
C10.228.140.079.612.800
C10.228.662.550.800
C10.574.625.800
Definition English:   A sporadic neurodegenerative disease with onset in middle-age characterized clinically by Parkinsonian features (e.g., MUSCLE RIGIDITY; HYPOKINESIA; stooped posture) and HYPOTENSION. This condition is considered a clinical variant of MULTIPLE SYSTEM ATROPHY. Pathologic features include a prominent loss of neurons in the zona compacta of the SUBSTANTIA NIGRA and PUTAMEN. (From Adams et al., Principles of Neurology, 6th ed, p1075-6) 
See Related English:   Parkinsonian Disorders
 
History Note English:   2000; use MULTIPLE SYSTEM ATROPHY 1998-1999 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RA radiography
RI radionuclide imaging RT radiotherapy
RH rehabilitation SU surgery
TH therapy US ultrasonography
UR urine VE veterinary
VI virology  
Record Number:   34222 
Unique Identifier:   D020955 

Occurrence in VHL:
 

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